RHD*16.02 - RHD*DCS2
(ISBT table: RHD partial D v5.0)
This entry is an RHD allele.
DCS-2, RHD(A226P), RHD*676C, RHD*676C (DCS2, RHD*16.02), RHD*676G>C,
Molecular data
Phenotype
Main D phenotype: weak D (last update: May 4, 2020)Reports by D phenotype
Other RH phenotypes: RH:-2, -5, -23,
Serology with monoclonal anti-D
Antigen Density (Ag/RBC)
More phenotype data
Rhesus Similarity Index
Haplotype
Main CcEe phenotype association: cE (last update: May 4, 2020)Alloimmunization
Antibodies in carriers
Antibody specificity: D (RH1)
Summary: no published cases (last update: Nov. 17, 2019)Detailed information
Antibodies in D negative recipients
Alloimmunization in recipients: expected to be possible, see phenotype data
Reports
Summary: rare descriptions, unclear descent (last update: Dec. 20, 2019)Detailed reports
- 2 samples related individuals Croatian
- 1/1274540 among donors with D negative or weak D phenotype, or patients with weak D phenotype (44 partial D types detailed, 149 weak D types not detailed) Shanghai Chinese
- 1/163 selected variants included for the development of a genotyping assay mainly in the Dutch population (samples may have been included in other studies)
- 1/100 donors with weak D phenotype Australia
Allele or phenotype frequency
Structure mapping
Movement | Mouse Input | Touch Input | ||
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Rotation | Primary Mouse Button | Single touch | ||
Translation | Middle Mouse Button or Ctrl+Primary | Triple touch | ||
Zoom | Scroll Wheel or Second Mouse Button or Shift+Primary | Pinch (double touch) | ||
Slab | Ctrl+Second | Not Available |
References
- Flegel WA et al. DCS-1, DCS-2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule. Transfusion, 2008. [Citation] [RHeference]
- Flegel WA et al. D variants at the RhD vestibule in the weak D type 4 and Eurasian D clusters. Transfusion, 2009. [Citation] [RHeference]
- Ye L et al. Partial D phenotypes and genotypes in the Chinese population. Transfusion, 2012. [Citation] [RHeference]
- Haer-Wigman L et al. RHD and RHCE variant and zygosity genotyping via multiplex ligation-dependent probe amplification. Transfusion, 2013. [Citation] [RHeference]
- McGowan EC et al. Diverse and novel RHD variants in Australian blood donors with a weak D phenotype: implication for transfusion management. Vox Sang, 2017. [Citation] [RHeference]
- Floch A et al. Comment from Rheference Online ressource, 2020. — Online ressource — [RHeference]
Last update: May 4, 2020